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. 2020 Oct 13;2020(10):CD013686. doi: 10.1002/14651858.CD013686.pub2

Timmerman 2004.

Study characteristics
Methods Trial design: RCT – split‐mouth design
Location: Centre for Dentistry, Amsterdam, the Netherlands
Setting: closed operatory room
Language: English
Number of centres: 1
Study period: not mentioned
Funding source: not mentioned
Study protocol: not available
Participants Age: 43 to 69 years
Total number of participants: 6 (3 male, 3 female)
Inclusion criteria:
  • patients who were referred to the Academic Centre for Dentistry in Amsterdam (ACTA) for diagnosis and treatment of periodontitis

  • patients who had at least 3 teeth in each quadrant

  • patients who were diagnosed as having generalized chronic periodontitis


Exclusion criteria: use of antibiotics or topical antiseptics during a period of 30 days prior to the study
Number randomized: 6
Number evaluated (withdrawals/missing participants): 6
Interventions Comparison: HVE versus conventional dental suction (low‐volume evacuator)
Intervention:
Group name: with HVE (high‐volume evacuation)
Number of intervention groups: 1
Number randomized to intervention group: 6
Description of intervention: the study included 17 treatment sessions, consisting of a 40‐minute episode of continuous plaque and calculus removal using an ultrasonic unit (EMS). The treatment sessions were carried out in 6 patients with generalized adult periodontitis and ranged from 2 to 4 sessions per patient according to their needs. The use of HVE and CDS was randomly assigned over the sessions within each patient. Before each treatment, the operating room was not used for 15 hours. To measure baseline microbial air pollution 2 Petri dishes containing blood agar were exposed for 10 minutes to the air. At the start of each treatment session, 2 Petri dishes were exposed for 5 minutes at a distance of 40 cm from the mouth of the patients. After 20 minutes, this procedure was repeated. At a distance of 150 cm, 2 Petri dishes were exposed for 20 minutes followed by exposure of 2 new Petri dishes for the rest of the session. The plates were cultured aerobically and anaerobically for 3 and 7 days, respectively
Any co‐interventions: no
Comparator:
Group name: with conventional dental suction (CDS)
Number of control groups: 1
Number randomized to control group: 6
Description of control: as described above
Outcomes Outcome name: reduction in contamination of aerosols
Outcome measurement: CFU (using blood agar plates), both aerobic and anerobic culture were done
Effect estimate: mean (SD)
Key conclusions: the results of the present study showed no differences when different methods of suction were used. This might indicate that the amount of aerosol with small particle size, able to carry bacteria over a larger distance, as produced by the present piezoelectric device, is relatively limited. The use of a high‐volume evacuator may, however, help to minimize risks of air microbial contamination.
Notes We contacted the study author for method of randomisation, allocation concealment, personnel blinding and study protocol. We sent an e‐mail on 26 July 2020 to the contact author and the e‐mail bounced back. We could not contact other authors as their e‐mail details are not available.
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk No details available
Allocation concealment (selection bias) Unclear risk No details available
Blinding of participants and personnel (performance bias)
All outcomes Low risk Blinding is not possible. However, participants and personnel will not be able to alter their behaviour even if they know the received intervention.
Blinding of outcome assessment (detection bias)
All outcomes Unclear risk It is not clear if the CFU were manually counted or any automated colony counters were used – there is subjectivity if manually counted.
Incomplete outcome data (attrition bias)
All outcomes Low risk Outcomes of all 6 participants are reported
Selective reporting (reporting bias) Unclear risk We are not sure of reporting selective outcomes as there is no protocol available
Other bias Low risk None